B. Braun Medical is recalling certain batches of 0.9% Sodium Chloride Injection due to potential microscopic leaks that could compromise sterility. Affected lots have specific expiration dates and NDC numbers.
Lack of sterility assurance: Recall of certain batches of 0.9% Sodium Chloride for Injection USP in EXCEL¿ Plus IV Container product due to the possibility of an incomplete seal that may cause leakage. The impacted lots may exhibit microscopic channel leaks near the port assembly of the product.
B. Braun Medical is recalling specific batches of 1000mL IV saline containers because they may have microscopic leaks near the port assembly. This could allow contamination, making the saline unsafe for medical use.
The recalled saline containers may have microscopic channel leaks near the port assembly. This could allow contaminants to enter the solution, potentially compromising sterility and causing infections if used in medical procedures.
Healthcare professionals and patients using the recalled saline products. Those who have the specific lot numbers listed in the recall are most at risk.
Check the product label for the NDC number 0264-5802-00 and lot numbers listed: 0061786962 through 0061826488. The expiration dates range from November 30, 2023 to August 31, 2024.
Look for the NDC number 0264-5802-00 and lot numbers between 0061786962 and 0061826488 on the container.
The recall is due to the possibility of microscopic channel leaks near the port assembly that could compromise sterility.
Check the product label for the NDC number 0264-5802-00 and lot numbers listed. If you have the affected lots, contact B. Braun Medical for guidance.
The recall indicates a potential sterility issue, but no specific injuries have been reported. The risk is low as the leaks are microscopic and may not cause immediate harm.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall D-0346-2023 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall D-0346-2023 from B. Braun Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
